A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv963498



Internal ID16257454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:61147025..61200876hg38UCSC Ensembl
Innerchr3:61132698..61186550hg19UCSC Ensembl
Innerchr3:61107738..61161590hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3853852
hg1953853
hg1853853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590425
Supporting Variants
Samples
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv963498
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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